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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 351150생성일: 2026년 10월 23일

Methyl 1-benzyl-5-oxopyrrolidine-3-carboxylate → (1-Benzylpyrrolidin-3-yl)methanol

https://huagongshe.com/ko/reaction/351150

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 1-benzyl-5-oxopyrrolidine-3-carboxylateHCID 98909—
반응물Aluminium lithium hydrideHCID 21226445—
용매Diethyl EtherHCID 3283—
생성물(1-Benzylpyrrolidin-3-yl)methanolHCID 5176654—

반응 조건

온도0 °C

반응 단계

First, N-benzyl-pyrrolidine-3-methanol was prepared as follows. Methyl N-benzyl-5-oxo-pyrrolidine-3-carboxylate (11.66 g, 50 mmol) was dissolved in diethyl ether and cooled to 0° C. This solution was added to a 0° C. suspension of lithium aluminum hydride in diethyl ether under nitrogen atmosphere. After addition, the mixture was refluxed for 1 hr. and then cooled with an ice bath. To quench the reaction, sodium sulfate decahydrate was added and the mixture was stirred for 1 hr. After filtration, the filtrate was collected, and concentrated to dryness to give N-Benzyl-pyrrolidine-3-methanol. ESMS (C12H17NO): calcd. 191.13; obsd. 192–2 [M+H]+. Retention time (anal. HPLC: 10–70% MeCN/H2O over 5 min)=0.95 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07183323B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-4af4207eaf724d55ac7e72631be3c989
출처 메모uspto-grants-2007_02